You Searched For: Boc-D-Pro-OH


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Supplier: Ambeed
Description: (2S,4R)-4-Aminopyrrolidine-2-carboxylic acid, 4-BOC, N1-FMOC protected 97%

Supplier: Ambeed
Description: N-Boc-4-methylene-L-proline 97%

New Product

Supplier: ALADDIN SCIENTIFIC
Description: sBoc-D-Phe-Pro-OH is used as a reactant in the preparation of Phe-Pro-p-amidinobenzylamine analogs as potent and highly selective thrombin inhibitors.

New Product

Supplier: Ambeed
Description: (R)-1-Boc-4,4-Difluoropyrrolidine-2-carboxylic acid 97%

New Product

Supplier: BeanTown Chemical
Description: CAS: 84348-37-8; MDL No: MFCD01860669 Solid; Molecular Formula: C10H15NO5; MW: 229.24 Melting Point: 160° (decomposes) Optical Rotation: [α]22/D +19.0 to +23.0°, c = 0.5 in acetone

SDS

Catalog Number: (101854-182)
Supplier: Matrix Scientific
Description: Matrix Scientific Part Number: 042033-1G , MDL Number: MFCD04973957


Supplier: Ambeed
Description: (2S,4S)-1-(tert-Butoxycarbonyl)-4-fluoro-2-pyrrolidinecarboxylic acid 97%

Catalog Number: (AAH27225-03)
Supplier: Thermo Scientific Chemicals
Description: (2S,4S)-1-(tert-Butoxycarbonyl)-4-fluoro-2-pyrrolidinecarboxylic acid 97%

Catalog Number: (B-3930.0005BA)
Supplier: Bachem Americas
Description: These dipeptide building blocks containing Ser- or Thr-derived oxazolidines (pseudoprolines) proved to be versatile tools for overcoming some intrinsic problems in the field of peptide chemistry. The presence of pseudoprolines within a peptide sequence results in the disruption of β-sheet structures considered as a source of intermolecular aggregation during chain elongation, thus increasing solvation and coupling kinetics in peptide assembly. Therefore, use of pseudoprolines offer new possibilities for accessing large peptides by convergent strategies and chemoselective ligation techniques. Moreover, incorporation of a pseudoproline unit facilitates cyclization of peptides.


Catalog Number: (BT219455-1G)
Supplier: BeanTown Chemical
Description: CAS: 70138-72-6; MDL No: MFCD03419274 Solid; Molecular Formula: C10H18N2O3; MW: 214.26

SDS


Catalog Number: (B-4315.0005BA)
Supplier: Bachem Americas
Description: These dipeptide building blocks containing Ser- or Thr-derived oxazolidines (pseudoprolines) proved to be versatile tools for overcoming some intrinsic problems in the field of peptide chemistry. The presence of pseudoprolines within a peptide sequence results in the disruption of β-sheet structures considered as a source of intermolecular aggregation during chain elongation, thus increasing solvation and coupling kinetics in peptide assembly. Therefore, use of pseudoprolines offer new possibilities for accessing large peptides by convergent strategies and chemoselective ligation techniques. Moreover, incorporation of a pseudoproline unit facilitates cyclization of peptides.


Supplier: TCI America
Description: CAS Number: 203866-13-1
MDL Number: MFCD04973957
Molecular Formula: C10H16FNO4
Molecular Weight: 233.24
Purity/Analysis Method: >97.0% (GC,T)
Form: Crystal
Melting point (°C): 162
Specific rotation [a]20/D: -57 deg (C=1, MeOH)

SDS

Catalog Number: (B-4320.0005BA)
Supplier: Bachem Americas
Description: These dipeptide building blocks containing Ser- or Thr-derived oxazolidines (pseudoprolines) proved to be versatile tools for overcoming some intrinsic problems in the field of peptide chemistry. The presence of pseudoprolines within a peptide sequence results in the disruption of β-sheet structures considered as a source of intermolecular aggregation during chain elongation, thus increasing solvation and coupling kinetics in peptide assembly. Therefore, use of pseudoprolines offer new possibilities for accessing large peptides by convergent strategies and chemoselective ligation techniques. Moreover, incorporation of a pseudoproline unit facilitates cyclization of peptides.


Catalog Number: (B-4295.0005BA)
Supplier: Bachem Americas
Description: These dipeptide building blocks containing Ser- or Thr-derived oxazolidines (pseudoprolines) proved to be versatile tools for overcoming some intrinsic problems in the field of peptide chemistry. The presence of pseudoprolines within a peptide sequence results in the disruption of β-sheet structures considered as a source of intermolecular aggregation during chain elongation, thus increasing solvation and coupling kinetics in peptide assembly. Therefore, use of pseudoprolines offer new possibilities for accessing large peptides by convergent strategies and chemoselective ligation techniques. Moreover, incorporation of a pseudoproline unit facilitates cyclization of peptides.


Catalog Number: (77866-830)
Supplier: Ambeed
Description: (S)-1-(tert-Butoxycarbonyl)-3,3-dimethyl-4-oxopyrrolidine-2-carboxylic acid ≥95%

New Product


Catalog Number: (A-4210.0001BA)
Supplier: Bachem Americas
Description: Sequence: Boc-β-tBu-D-Ala-OH


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Stock for this item is limited, but may be available in a warehouse close to you. Please make sure that you are logged in to the site so that available stock can be displayed. If the call is still displayed and you need assistance, please call us at 1-800-932-5000.
This product is marked as restricted and can only be purchased by approved Shipping Accounts. If you need further assistance, email VWR Regulatory Department at Regulatory_Affairs@vwr.com
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